Colonic strictures in patients with cystic fibrosis: Results of a survey of 114 cystic fibrosis care centers in the United States

被引:29
作者
Freiman, JP
FitzSimmons, SC
机构
[1] CYST FIBROSIS FDN,BETHESDA,MD 20814
[2] US FDA,CTR DRUG EVALUAT & RES,OFF EPIDEMIOL & BIOSTAT,DIV EPIDEMIOL & SURVEILLANCE,ROCKVILLE,MD 20857
关键词
cystic fibrosis; pancreatic enzymes; colonic strictures;
D O I
10.1097/00005176-199602000-00005
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
We describe 15 cases of stricture of the colon requiring surgery in cystic fibrosis patients identified from a survey of 114 cystic fibrosis care centers in the United States. Patient ages ranged from 2 to 8 years, seven of the 15 patients were female. A history of meconium ileus was reported in nine of the 15 cases. Fibrosis of the submucosa was described in 14 surgical pathology reports. Pancreatic enzyme use history was available from 14 reports. All had taken delayed-release products for 6-96 months at average doses ranging from 6,700 to 29,100 units lipase/kg/meal, but only eight of them used products containing >20,000 units lipase per capsule prior to surgery.
引用
收藏
页码:153 / 156
页数:4
相关论文
共 50 条
  • [31] Airway Clearance Therapy in Cystic Fibrosis Patients Insights from a Clinician Providing Cystic Fibrosis Care
    Chaudary, Nauman
    Balasa, Gabriella
    INTERNATIONAL JOURNAL OF GENERAL MEDICINE, 2021, 14 : 2513 - 2521
  • [32] Cystic Fibrosis Transitions of Care Lessons Learned and Future Directions for Cystic Fibrosis
    Okumura, Megumi J.
    Kleinhenz, Mary Ellen
    CLINICS IN CHEST MEDICINE, 2016, 37 (01) : 119 - +
  • [33] Cystic fibrosis mutations and associated haplotypes in Turkish cystic fibrosis patients
    Onay, T
    Zielenski, J
    Topaloglu, O
    Gokgoz, N
    Kayserili, H
    Apak, MY
    Camcioglu, Y
    Cokugras, H
    Akcakaya, N
    Tsui, LC
    Kirdar, B
    HUMAN BIOLOGY, 2001, 73 (02) : 191 - 203
  • [34] Adult Care in Cystic Fibrosis
    Elborn, J. Stuart
    SEMINARS IN RESPIRATORY AND CRITICAL CARE MEDICINE, 2019, 40 (06) : 857 - 868
  • [35] Cystic fibrosis transmembrane regulator haplotypes in households of patients with cystic fibrosis
    Furgeri, Daniela Tenorio
    Lima Marson, Fernando Augusto
    Araujo Correia, Cyntia Arivabeni
    Ribeiro, Jose Dirceu
    Bertuzzo, Carmen Silvia
    GENE, 2018, 641 : 137 - 143
  • [36] Transitions of Care in Cystic Fibrosis
    DeFilippo, Eunice M. M.
    Talwalkar, Jaideep S.
    Harris, Zachary M.
    Butcher, Jennifer
    Nasr, Samya Z.
    CLINICS IN CHEST MEDICINE, 2022, 43 (04) : 757 - 771
  • [37] The globalization of cystic fibrosis care
    Milla, Carlos E.
    CURRENT OPINION IN PEDIATRICS, 2025, 37 (03) : 266 - 271
  • [38] When is cystic fibrosis not cystic fibrosis? The importance of appropriately classifying patients
    Faro, Albert
    Goss, Christopher
    Cromwell, Elizabeth
    Elbert, Alex
    Brown, Anne W.
    Marshall, Bruce C.
    RESPIRATORY MEDICINE, 2022, 193
  • [39] First report of cystic fibrosis mutations in Libyan cystic fibrosis patients
    Fredj, Sondess Hadj
    Fattoum, Slaheddine
    Chabchoub, Abdelraouf
    Messaoud, Taieb
    ANNALS OF HUMAN BIOLOGY, 2011, 38 (05) : 561 - 563
  • [40] Nebulizers in cystic fibrosis: a source of bacterial contamination in cystic fibrosis patients?
    Costa Brzezinski, Lorena Xavier
    Riedi, Carlos Antonio
    Kussek, Paulo
    de Melo de Souza, Helena Homem
    Rosario, Nelson
    JORNAL BRASILEIRO DE PNEUMOLOGIA, 2011, 37 (03) : 341 - 347